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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2200768Generated: October 30, 2026

Methanesulfonyl chloride → HCID 178505326, compound

https://huagongshe.com/reaction/2200768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 178521599HCID 178521599—
SolventDichloromethaneHCID 6344—
ProductHCID 178505326HCID 178505326—

Reaction Steps

As shown in step 6-ii of Scheme 6, to compound 1013 (1.2 g, 4.41 mmol) in DCM (20 mL) was added TEA (1.134 g, 1.84 mL, 13.2 mmol) and MsCl (505 mg, 341 μL, 4.41 mmol). The reaction mixture was stirred for 1 hour, concentrated under reduced pressure, and purified by medium pressure silica gel chromatography (0 to 80% EtOAc/hexanes gradient) to provide trans-4-((5-bromopyrimidin-2-yl)amino)cyclohexyl methanesulfonate (compound 1014): 1H-NMR (300 MHz, CDCl3) δ 8.29 (s, 2H), 5.03 (d, J=7.8 Hz, 1H), 4.70 (tt, J=10.6, 3.9 Hz, 1H), 3.80 (dtt, J=11.2, 7.6, 3.7 Hz, 1H), 3.04 (s, 3H), 2.30-2.12 (m, 4H), 1.93-1.69 (m, 2H), 1.51-1.33 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359380B2
Source datasetuspto-grants-2016_06
ORD IDord-8f0078a2f89d4b839f602534cc2cce81
Source noteuspto-grants-2016_06